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PRidopidine's Outcome On Function in Huntington Disease, PROOF- HD

Sponsored by Prilenia

About this trial

Last updated 2 years ago

Study ID

PL101-HD301

Status

Active, not recruiting

Type

Interventional

Phase

Phase 3

Placebo

Yes

Accepting

18-75 Years
25+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 years ago

What is this trial about?

This study will evaluate the efficacy and safety of pridopidine 45mg twice daily (BID) in patients with early stage manifest Huntington Disease (HD).

What are the Participation Requirements?

INCLUSION CRITERIA MAIN STUDY

1. Diagnosis of HD based on clinical features and the presence of ≥36 CAG repeats in the
huntingtin gene

2. Diagnostic confidence level (DCL) of 4

3. Adult-onset HD with onset of signs and symptoms ≥18 years of age

4. Stage 1 or Stage 2 HD, defined as a UHDRS-TFC score of ≥7, at screening

EXCLUSION CRITERIA

1. Use of pridopidine within 12 months before the baseline visit.

2. Gene therapy at any time

3. Any serious medical condition or clinically significant laboratory, or vital sign
abnormality that precludes the patient's safe participation in and completion of the
study e.g. significant heart disease within 12 weeks before baseline or history of
certain cardiac arrhythmias

4. History of epilepsy or seizures within the last 5 years

5. Pregnant or breastfeeding, or intention to become pregnant during the study

Locations

Location

Status